Xenco Medical, LLC is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Xenco Medical, LLC - FDA 510(k) Cleared Devices
Recent clearances: Xenco Medical CancelleX Cervical Interbody System, Xenco Medical InterAlign Cervical Interbody System, Xenco Medical Multilevel CerviKit
16
Total
16
Cleared
0
Denied
Xenco Medical, LLC has 16 FDA 510(k) cleared orthopedic devices. Based in San Diego, US.
Latest FDA clearance: Jan 2025. Active since 2014.
Browse the complete list of FDA 510(k) cleared orthopedic devices from this manufacturer. Filter by specialty or product code using the sidebar.
Regulatory submissions have been managed by Secure BioMed Evaluations, KARA & Associates and Converg Engineering, LLC.
FDA 510(k) Regulatory Record - Xenco Medical, LLC
16 devices
Cleared
Jan 29, 2025
Xenco Medical CancelleX Cervical Interbody System
Orthopedic
63d
Cleared
Jun 07, 2023
Xenco Medical InterAlign Cervical Interbody System
Orthopedic
250d
Cleared
Dec 21, 2021
Xenco Medical Multilevel CerviKit
Orthopedic
56d
Cleared
Sep 27, 2019
Sorrento Bone Graft Substitute
Orthopedic
157d
Cleared
Apr 18, 2019
CancelleX Porous Titanium Lumbar Interbody Device
Orthopedic
62d
Cleared
Sep 13, 2018
Sorrento Bioglass Bone Graft Substitute
Orthopedic
261d
Cleared
Aug 24, 2018
CancelleX Porous Titanium Lumbar Interbody Device
Orthopedic
193d
Cleared
May 25, 2017
SETx Pedicle Screw System
Orthopedic
85d
Cleared
Oct 21, 2016
Xenco Medical Cervical Interbody System
Orthopedic
259d
Cleared
Sep 06, 2016
Xenco Medical Posterior Cervical System
Orthopedic
98d
Cleared
May 04, 2016
Xenco Medical Pedicle Screw System
Orthopedic
26d
Cleared
Dec 11, 2015
Xenco Medical Cervical Interbody System, Xenco Medical Lumbar Interbody System
Orthopedic
59d